Please note that this event is already in progress or has finished.
It might be possible to obtain information from the organiser about similar future events
[or if available notes/abstract from this meeting].
Please check out any links below - if these are not of any help then contact the organiser using the "Inquire" button below.
Go to current meetings
Date: 17th - 18th August, 2009
Location: Malvern, PA , USA
Summary:Pharmaceutical - Training
This is a course for people who must write process documents required by the binding regulations. Process documents in sum create a procedural infrastructure that delineates the company’s activities. These documents include Standard Operating Procedures (SOPs); policies; work instructions; laboratory methods; emergency action, chemical hygiene, animal husbandry and other plans; and quality manuals. This course is valuable for pharmaceutical, medical device, and biotech professionals in drug discovery, product development, quality assurance, clinical testing, information technology, and regulatory affairs. It is also helpful for senior and middle management executives who want to familiarize themselves with the regulations that mandate procedures and the industry standards for writing them, putting them in place, and remaining compliant.
Writing Effective Standard Operating Procedures and Other Process Documents